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We write when we can, Susie. I hope you'll join in as often as you can.

There is no special time. There is mail on here just about all the time. We can

read, or ask our questions, just talk, or fuss about your caregiver load. We

take it all in stride and help each other no end! It is something else at the

things I have learned since I have been here. I haven't been on too very

long either.

This is a great group of wonderful people. We all know we are under more

stress than three people should have, so we try to support each other all we

can. If we step on toes, it sure isn't intentional.

We have the best run list I have even encountered. Easy going, and kind.

Enjoy anytime you wish, Susie.

Imogene

Caregiver for my True Texas Gentleman husband of 35 years. He has LBD with

Parkinsonism, and Frontal Lobe Disease with Apathy, and possibly AD.

Love is Long-suffering---- love never fails 1 Cor. 13; 4-7 (Paraphrased for

caregivers)

In a message dated 6/15/2006 8:03:50 PM Central Daylight Time,

gentlysm06@... writes:

Is there a special time that caregivers are chatting? what do I need to

do to access that? Thanks for your help. Susie

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Since I've been on this board (since January) there hasn't been a chat

within this group that I'm aware of. With that said, in the links

section of our board there is a link about a LBDCaregivers chat room

that someone started - don't know if it's something that still happens

or not... Click here for details:

http://health.groups.yahoo.com/group/LBDcaregivers/links/Caregiver_Suppo

rt_001149946133/

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I looked at this, . I was quite pleased. I will try to look into the

various sites, and chats. I was especially happy to find a section on

stress.

Thank you very much,

Imogene

Caregiver for my True Texas Gentleman husband of 35 years. He has LBD with

Parkinsonism, and Frontal Lobe Disease with Apathy, and possibly AD.

Love endures all things---- love never fails 1 Cor. 13; 4-7 (Paraphrased for

caregivers)

In a message dated 6/16/2006 5:37:00 AM Central Daylight Time,

octoryrose@... writes:

Since I've been on this board (since January) there hasn't been a chat

within this group that I'm aware of. With that said, in the links

section of our board there is a link about a LBDCaregivers chat room

that someone started - don't know if it's something that still happens

or not... Click here for details:

http://health.groups.yahoo.com/group/LBDcaregivers/links/Caregiver_Suppo

rt_001149946133/

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I have forward this message to Sandy. She use to have the chat going and I

don't know if anyone is still there or not. If anyone is interested, I know she

had a site.

Donna R

Do you want to read more about Lewy Body? You can also read the Thistle, the LBD

Newsletter. Just click on:

http://www.lewybodydementia.org

Re: chat

Since I've been on this board (since January) there hasn't been a chat

within this group that I'm aware of. With that said, in the links

section of our board there is a link about a LBDCaregivers chat room

that someone started - don't know if it's something that still happens

or not... Click here for details:

http://health.groups.yahoo.com/group/LBDcaregivers/links/Caregiver_Suppo

rt_001149946133/

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  • 3 years later...

Alright you guys, it's another new week, so I am sending you all a

semi-private invitation...... Click HERE <http://www.asap.org/chat.html> in

50 minutes to come to chat! There is a back-up chat

site<http://www.chatmaker.net/chatap/rooms/chiari/>too since asap's

site has been acting weird. But try the first link FIRST.

Just click on the links.....

See ya there!

Me Chele

--

To read all about Chiari, go to http://www.asap.org/

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